Cleared Traditional

Pac-Dent Denture Base Resin (K210189) - FDA 510(k) Clearance

Class II Dental device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K210189 · Pac-Dent, Inc. · Dental device
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Jul 2021
Decision
184d
Days
Class 2
Risk

K210189 is an FDA 510(k) clearance for the Pac-Dent Denture Base Resin. Classified as Resin, Denture, Relining, Repairing, Rebasing (product code EBI), Class II - Special Controls.

Submitted by Pac-Dent, Inc. (Brea, US). The FDA issued a Cleared decision on July 28, 2021 after a review of 184 days - an extended review cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3760 - the FDA dental device regulatory framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Dental review framework, consistent with the majority of Class II 510(k) submissions.

View all Pac-Dent, Inc. devices

Submission Details

510(k) Number K210189 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 25, 2021
Decision Date July 28, 2021
Days to Decision 184 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
57d slower than avg
Panel avg: 127d · This submission: 184d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code EBI Resin, Denture, Relining, Repairing, Rebasing
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3760
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Dental devices follow this clearance model.

Regulatory Peers - EBI Resin, Denture, Relining, Repairing, Rebasing

All 111
Devices cleared under the same product code (EBI) and FDA review panel - the closest regulatory comparables to K210189.
Glidewell 3DP Denture Base Resin
K213765 · Prismatik Dentalcraft, Inc. · Jun 2022
Flexible Block
K213994 · Shandong Huge Dental Material Corporation · Mar 2022
3Delta Denture Base - 3Delta Denture Bond - 3Delta Denture Fix
K212541 · Deltamed GmbH · Jan 2022
GR-14 Resin System
K210298 · Pro3dure Medical GmbH · May 2021
E-Denture Pro
K203641 · Envisiontec GmbH · Mar 2021
DIOnavi-Denture02
K210828 · Dio Corporation · Mar 2021